EP1125941B1 - Dérivés d'acides 6-sulfamoyl-3-quinolyl phosphoniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent - Google Patents

Dérivés d'acides 6-sulfamoyl-3-quinolyl phosphoniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent Download PDF

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Publication number
EP1125941B1
EP1125941B1 EP01400408A EP01400408A EP1125941B1 EP 1125941 B1 EP1125941 B1 EP 1125941B1 EP 01400408 A EP01400408 A EP 01400408A EP 01400408 A EP01400408 A EP 01400408A EP 1125941 B1 EP1125941 B1 EP 1125941B1
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EP
European Patent Office
Prior art keywords
formula
compound
compounds
pharmaceutically acceptable
defined hereinbefore
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EP01400408A
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German (de)
English (en)
French (fr)
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EP1125941A1 (fr
Inventor
Alex Cordi
Patrice Desos
Pierre Lestage
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Laboratoires Servier SAS
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Laboratoires Servier SAS
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/576—Six-membered rings
    • C07F9/60—Quinoline or hydrogenated quinoline ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention relates to new derivatives of 6-sulfamoyl-3-quinolinyl acids phosphonic acid, process for their preparation and the compositions containing them.
  • Patent EP0640612 describes compounds capable of opposing the excitatory and toxic effects of excitatory amino acids (AAE) by blocking the initial activation of the PAMPA receptor ( ⁇ -amino-3-hydroxy-5-methyl-4-isoxazole acid- propionic) / kainate. Their utility is thus recognized for inhibiting pathological phenomena, in particular neurotoxic ones linked to the hyperactivation of the neurotransmission pathways to excitatory amino acids.
  • non-limiting examples that may be mentioned sodium hydroxide, potassium hydroxide, triethylamine, tertbutylamine, etc.
  • the preferred compounds of the invention are the compounds of formula (I) for which R represents a hydrogen atom.
  • the invention also extends to the process for preparing the compounds of formula (I) characterized in that a compound of formula (II) is used as starting material: in which X is as defined in formula (I), on which is condensed in the presence of a base such as pyridine for example a compound of formula (III): to lead to the compound of formula (IV): in which X is as defined above, which is cyclized in the presence of a catalytic amount of piperidine to obtain the compound of formula (V): where X is defined as above, which is subjected to a mixture of nitric acid and sulfuric acid to yield the compound of formula (VI): in which X is as defined above, which is reduced by using palladium-on-carbon in the presence of hydrogen or iron in a hydroalcoholic medium to obtain the compound of formula (VII): where X is defined as above, which is subjected, after transformation into the corresponding diazonium salt, to the action of sulfur dioxide in the presence of CuCl 2 to yield the compound of
  • the compounds of the invention have quite pharmacological properties interesting since they are powerful inhibitors of the AMPA receptor, moreover selective since they do not touch the NMDA receptor and are therefore devoid of all side effects described for NMDA antagonists, and especially devoid of the nephrotoxicity associated with a number of AMPA / non-NMDA antagonists.
  • the use of these compounds as inhibitors of pathological phenomena linked to hyperactivation of neurotransmission pathways to excitatory amino acids will thus be particularly appreciated in acute and especially chronic treatments of neurological diseases and psychic involving these amino acids like degenerative diseases such as stroke, cerebral or spinal trauma, epilepsy, diseases chronic neurodegenerative diseases such as Alzheimer's disease, schizophrenia, amyotrophic lateral sclerosis or Huntington's chorea.
  • the present invention also relates to pharmaceutical compositions containing as active principle at least one compound of formula (I) alone or in combination with one or more pharmaceutically acceptable excipients.
  • compositions according to the invention there may be mentioned more especially those suitable for oral, parenteral, nasal, per or transcutaneous, rectal, perlingual, ocular or respiratory and in particular the tablets single or coated, sublingual tablets, sachets, packages, capsules, glossettes, tablets, suppositories, creams, ointments, dermal gels and drinkable or injectable ampoules.
  • the dosage varies according to the patient's sex, age and weight, the route of administration, the nature of the therapeutic indication, or possibly associated treatments and ranges from 50 mg to 1 g per 24 hours in 1 or more doses.
  • a suspension of the compound obtained in stage C (7.0 g, 19.4 mmol), iron powder (10.8 g, 194 mmol), and ammonium chloride (10.4 g, 194 mmol) is stirred at reflux for 1 hour in a mixture of 270 ml of methanol and 90 ml of water.
  • the suspension is filtered hot on celite and the solid is rinsed several times with methanol.
  • the filtrate is evaporated to dryness and the residue is taken up in suspension in water.
  • the solid is filtered, rinsed with water and dried to obtain the title product in the form of orange crystals. Melting point : 255-260 ° C
  • Elementary microanalysis VS% H% NOT% calculated 47 , 22 4 , 88 8 , 47 find 47 , 06 4 , 99 8, 08
  • a solution of 13.4 ml of acetic acid and 2.25 ml of water is saturated with SO 2 by bubbling SO 2 gas for 15 minutes.
  • a solution of the compound obtained in Stage D (3.34 g, 10.1 mmol) in a mixture of 10 ml of glacial acetic acid and 17 ml of concentrated HCl is prepared at 5 ° C.
  • To this solution is added dropwise a solution of sodium nitrite (767 mg, 11.11 mmol) previously dissolved in 5 ml of water and the reaction is stirred for 30 minutes at 5 ° C.
  • To the saturated SO 2 solution is added CuCl 2 .2H 2 O (689 mg, 4.04 mmol) and the suspension obtained is cooled to 5 ° C.
  • Stage G (7 -chloro -2 -oxo -6-sulfamoyl-1,2-dihydro-3-quinolinyl) phosphonic acid
  • Example 2 The procedure is as in Example 1, replacing in stage A 2-amino-4-chlorobenzaldehyde with 2-amino-4-trifluoromethyl-benzaldehyde and carrying out the reduction step in stage D with the pair Pd-C / ammonium formate instead of the Fe / NH 4 Cl pair in an alcoholic medium.
  • Stage F Acid (7-trifluoromethyl-2-oxo-6-sulfamoyl-1,2-dihydro-3 -quinolinyl) phosphonic diethyl ester
  • Uninsulated product (oil) used as is in stage B.
  • Stage F Acid (7-fluoro-2 -oxo-6-sulfamoyl-1,2-dihydro-3-quinolinyl) phosphonic diethyl ester
  • EXAMPLEA Inhibition of the current induced by an application of (R, S) -AMPA (10 ⁇ M) on Xenope oocytes injected with mRNA of rat cortex
  • Xenopes oocytes are injected with 50 ng of poly (A +) mRNA isolated from rat cerebral cortex and incubated 2 to 3 days at 18 ° C to allow protein expression.
  • the products of the present invention are applied in a dependent concentration 30 seconds before and during the application of the agonist (R, S) -AMPA.
  • the compounds of the invention show excellent inhibitory properties with IC50 ( ⁇ M) of the order of 0.1.
  • seizures may be triggered by subjecting this animal to high intensity and high frequency sound stimulation.
  • AMPA-type glutamate receptor antagonists antagonize this type of seizure in a dose-dependent manner (Chapman et al., Epilepsy Res., 1991, 9 , 92-96).
  • This test is used to study the anti-convulsant effects of the compounds of the present invention. Briefly, immature DBA / 2 mice (21-28 days) are exposed for 60 seconds to 105 dB and 18 kHz noise. This leads to the appearance of clonic convulsions. The products under study and the solvent are administered ip 30 minutes before the start of the test in a volume of 0.1 ml / 10 g.
  • the ED50 doses inhibiting by 50% the incidence of convulsions is determined for each compound using the method of Litchfield and Wicoxon (J. Pharmacol. Exp. Ther., 1949, 96 , 99-113).
  • the compounds of the invention show an excellent ability to inhibit convulsions with ED50s of the order of 3 mg / kg ip.
  • the evaluation of the renal impact of the compounds of the present invention is carried out in the adult male Fischer rat of 200-250 g. Fischer rats are anesthetized with pentobarbital (Nembutal®, 60 mg / kg i.p.). Ninety minutes after induction of anesthesia, the compounds under study are administered intravenously at doses of 3, 10 and 15 mg / kg. Twenty-four hours after administration, the animals are sacrificed, the plasma is taken and serum creatinine and uremia are measured. Statistical analysis is carried out at using a factor analysis of variance followed by a Newman-Keuls test, in comparing the treated animals and the animals having only received the vehicle.
  • the compounds of the invention have excellent renal tolerance, no effect toxic only obtained for doses less than or equal to 15 mg / kg iv.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Psychiatry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Epidemiology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
EP01400408A 2000-02-18 2001-02-16 Dérivés d'acides 6-sulfamoyl-3-quinolyl phosphoniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent Expired - Lifetime EP1125941B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0002011 2000-02-18
FR0002011A FR2805260A1 (fr) 2000-02-18 2000-02-18 Nouveaux derives d'acides 6-sulfamoyl-3-quinolinyl phosphoniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Publications (2)

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EP1125941A1 EP1125941A1 (fr) 2001-08-22
EP1125941B1 true EP1125941B1 (fr) 2003-04-09

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EP01400408A Expired - Lifetime EP1125941B1 (fr) 2000-02-18 2001-02-16 Dérivés d'acides 6-sulfamoyl-3-quinolyl phosphoniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent

Country Status (20)

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US (2) US6518258B1 (zh)
EP (1) EP1125941B1 (zh)
JP (1) JP2001253892A (zh)
KR (1) KR20010082703A (zh)
CN (1) CN1317490A (zh)
AR (1) AR027429A1 (zh)
AT (1) ATE236911T1 (zh)
AU (1) AU2304001A (zh)
BR (1) BR0100604A (zh)
CA (1) CA2337786A1 (zh)
DE (1) DE60100165D1 (zh)
EA (1) EA200100156A3 (zh)
FR (1) FR2805260A1 (zh)
HK (1) HK1039619A1 (zh)
HU (1) HUP0100750A3 (zh)
MX (1) MXPA01001558A (zh)
NO (1) NO20010800L (zh)
NZ (1) NZ510001A (zh)
PL (1) PL345918A1 (zh)
ZA (1) ZA200101338B (zh)

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PT1871368E (pt) * 2005-04-04 2011-08-30 Eisai R&D Man Co Ltd COMPOSTOS DE DIHIDROPIRIDINA PARA DOENÇAS NEURODEGENERATIVAS E DEMjNCIA

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2683818B1 (fr) * 1991-11-14 1993-12-31 Adir Cie Nouveaux derives de 3-sulfonylamino-2-(1h)-quinoleinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
US5342946A (en) * 1992-12-02 1994-08-30 Guilford Pharmaceuticals Inc. Phosphonoalkylquinolin-2-ones as novel antagonists of non-NMDA ionotropic excitatory amino acid receptors
FR2709489B1 (fr) * 1993-08-31 1995-10-20 Adir Nouveaux dérivés de 2-(1H)-quinoléinone, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
FR2750988B1 (fr) * 1996-07-11 1998-09-18 Adir Nouveaux derives de 2-(1h)-quinoleinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
FR2805261A1 (fr) * 2000-02-18 2001-08-24 Adir Nouveaux derives d'acides 6-amino ou 6-hydrazinosulfonyl-3- quinolinyl phosphoniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
FR2805262A1 (fr) * 2000-02-18 2001-08-24 Adir Nouveaux derives d'acides aryle ou heteroaryle quinolinyl phosphoniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

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Publication number Publication date
CA2337786A1 (fr) 2001-08-18
ATE236911T1 (de) 2003-04-15
HUP0100750A2 (hu) 2002-01-28
EA200100156A3 (ru) 2001-10-22
KR20010082703A (ko) 2001-08-30
PL345918A1 (en) 2001-08-27
US6518258B1 (en) 2003-02-11
ZA200101338B (en) 2001-08-21
US6596709B1 (en) 2003-07-22
EP1125941A1 (fr) 2001-08-22
NO20010800L (no) 2001-08-20
NZ510001A (en) 2002-11-26
NO20010800D0 (no) 2001-02-16
HUP0100750A3 (en) 2002-09-30
AR027429A1 (es) 2003-03-26
BR0100604A (pt) 2001-09-18
AU2304001A (en) 2001-08-23
MXPA01001558A (es) 2002-08-06
EA200100156A2 (ru) 2001-08-27
JP2001253892A (ja) 2001-09-18
CN1317490A (zh) 2001-10-17
HK1039619A1 (zh) 2002-05-03
DE60100165D1 (de) 2003-05-15
HU0100750D0 (en) 2001-04-28
FR2805260A1 (fr) 2001-08-24

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